Linked Data
dbSNP Id:
rs1602325388
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.26607959T>G , CM000684.2:g.26607959T>G | GRCh38 |
| NC_000022.10:g.27003923T>G , CM000684.1:g.27003923T>G | GRCh37 |
| NC_000022.9:g.25333923T>G | NCBI36 |
| NG_009826.1:g.15069A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647569.1:n.174A>C | ||
| ENST00000647684.1:c.362A>C MANE Select | ENSP00000497249.1:p.Tyr121Ser | |
| ENST00000215939.2:c.362A>C | ENSP00000215939.2:p.Tyr121Ser | |
| NM_001887.3:c.362A>C | NP_001878.1:p.Tyr121Ser | |
| XM_011529899.1:c.362A>C | XP_011528201.1:p.Tyr121Ser | |
| NM_001887.4:c.362A>C MANE Select | NP_001878.1:p.Tyr121Ser | |
| XM_011529899.3:c.362A>C | XP_011528201.1:p.Tyr121Ser |